With Fermion, start the journey of your innovative API.
01 1Fermion Oy
02 1Excella GmbH & Co. K.G.
03 2HUZHOU ZHANWANG PHARMACEUTICAL CO. ,LTD
01 4Methotrexate
01 2China
02 1Finland
03 1Luxembourg
With Fermion, start the journey of your innovative API.
Registration Number : 219MF10359
Registrant's Address : Koivu-Mankkaan tie 6A, FI-02200 Espoo, Finland
Initial Date of Registration : 2007-12-13
Latest Date of Registration : 2018-05-15
Registration Number : 219MF10360
Registrant's Address : NUERNBERGER STRASSE 12, 90537 FEUCHT, GERMANY
Initial Date of Registration : 2007-12-13
Latest Date of Registration : 2024-11-27
Registration Number : 220MF10179
Registrant's Address : West Development Area, Linghu Town, Huzhou City, 313018, Zhejiang Province, China
Initial Date of Registration : 2008-07-31
Latest Date of Registration : 2018-03-14
Registration Number : 229MF10125
Registrant's Address : West Development Area, Linghu Town, Huzhou City, 313018, Zhejiang Province, China
Initial Date of Registration : 2017-07-14
Latest Date of Registration : 2017-07-14
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PharmaCompass offers a list of Methotrexate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Methotrexate manufacturer or Methotrexate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Methotrexate manufacturer or Methotrexate supplier.
PharmaCompass also assists you with knowing the Methotrexate API Price utilized in the formulation of products. Methotrexate API Price is not always fixed or binding as the Methotrexate Price is obtained through a variety of data sources. The Methotrexate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A RASUVO manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RASUVO, including repackagers and relabelers. The FDA regulates RASUVO manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RASUVO API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of RASUVO manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A RASUVO supplier is an individual or a company that provides RASUVO active pharmaceutical ingredient (API) or RASUVO finished formulations upon request. The RASUVO suppliers may include RASUVO API manufacturers, exporters, distributors and traders.
click here to find a list of RASUVO suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The RASUVO Drug Master File in Japan (RASUVO JDMF) empowers RASUVO API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the RASUVO JDMF during the approval evaluation for pharmaceutical products. At the time of RASUVO JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of RASUVO suppliers with JDMF on PharmaCompass.
We have 3 companies offering RASUVO
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